Superstrate CuInSe2-Printed Solar Cells on In2S3/TiO2/FTO/Glass Plates

CuInSe2 powders synthesized by ball milling were printed on In2S3/TiO2/FTO/glass substrates, resulting in superstrate solar cells.  Although particle structure of CuInSe2 in the layer remained after heating at 600 °C under N2 gas, photovoltaic effects were observed; the open-circuit voltage and short-circuit current density were 0.45 V and 5.6 mA/cm2, respectively.  The effects of annealing time on the structural, optical and photovoltaic properties of CuInSe2 were studied by scanning electron micrograph (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and UV-Vis reflectance absorption spectroscopy.  The CuInSe2 solar cells were printed in air ambient without vacuum processing and without toxic and explosive chemicals (e.g., hydrazine, H2Se and H2S), which can offer a promising strategy for future research and industrial investigation into cost-effective photovoltaic systems.Key words: Photovoltaic system; Photovoltaic effects; CuInSe2 solar cell

pH-Responsive Aqueous Bubbles Stabilized With Polymer Particles Carrying Poly(4-vinylpyridine) Colloidal Stabilizer

Free radical dispersion polymerization was conducted to synthesize near-monodispersed, micrometer-sized polystyrene (PS) particles carrying pH-responsive poly(4-vinylpyridine) (P4VP) colloidal stabilizer (P4VP-PS particles). The P4VP-PS particles were extensively characterized in terms of morphology, size, size distribution, chemical composition, surface chemistry, and pH-response using optical and scanning electron microscopies, elemental microanalysis, X-ray photoelectron spectroscopy, laser diffraction particle size analysis, and zeta potential measurement. The P4VP-PS particles can work as a pH-responsive stabilizer of aqueous bubbles by adsorption at the air-water interface. At and above pH 4.0, where the particles have partially protonated/non-protonated P4VP stabilizer with relatively hydrophobic character, particle-stabilized bubbles were formed. Optical and scanning electron microscopy studies confirmed that the P4VP-PS particles were adsorbed at the air-water interface of the bubbles in aqueous media. At and below pH 3.0, where the particles have cationic P4VP stabilizer with water-soluble character, no bubble was formed. Rapid disruption of the bubbles can be induced by decreasing the pH; the addition of acid caused the in situ protonation of pyridine groups in P4VP, which impart water-soluble character to the P4VP stabilizer, and the P4VP-PS particles were desorbed from the air-water interface. The bubble stabilization/destabilization cycles could be repeated at least five times

Soft-templated synthesis of mesoporous nickel oxide using poly(styrene-block-acrylic acid-block-ethylene glycol) block copolymers

In this work, we report the soft-templated preparation of mesoporous nickel oxide using an asymmetric poly(styrene-block-acrylic acid-block-ethylene glycol) (PS-b-PAA-b-PEG) triblock copolymer. This block copolymer forms a micelle consisting of a PS core, a PAA shell and a PEG corona in aqueous solutions, which can serve as a soft template. Specifically, the PS block forms the core of the micelles on the basis of its lower solubility in water. The anionic PAA block interacts with the cationic Ni ions present in the solution to generate the shell. The PEG block forms the corona of the micelles and stabilizes the micelles by preventing secondary aggregation through steric repulsion between the PEG chains. In terms of textural characteristics, the as-synthesized mesoporous NiO exhibits a large average pore size of 35 nm with large specific surface area and pore volume of 97.0 m g and 0.411 cm g, respectively. It is expected that the proposed soft-templated strategy can be expanded to other metal oxides/sulfides in the future for potential applications in gas sensors, catalysis, energy storage and conversion, optoelectronics, and biomedical applications

A New Year’s Message 2023

We wish you all happiness, health and progress in the new year [...

A New Year’s Message 2022

We greatly appreciate the contribution of Editorial Board Members, Guest Editors, reviewers, authors, and all related colleagues over the past year [...

Self-Assembly of Cholesterol-Containing Water-Soluble Polymers

Self-assembly of amphiphilic polymers containing cholesteryl groups has proved to be attractive in the field of nanotechnology research. Some cholesterol derivatives are known to form ordered structures which indicate thermotropic and lyotropic liquid-crystalline, monolayers, multilayers, micelles, and liposomes. This paper involves the synthesis and characterization of various kinds of amphiphilic polymers bearing cholesteryl moieties

Preparation of Water-soluble Polyion Complex (PIC) Micelles Covered with Amphoteric Random Copolymer Shells with Pendant Sulfonate and Quaternary Amino Groups

An amphoteric random copolymer (P(SA)91) composed of anionic sodium 2-acrylamido-2-methylpropanesulfonate (AMPS, S) and cationic 3-acrylamidopropyl trimethylammonium chloride (APTAC, A) was prepared via reversible addition-fragmentation chain transfer (RAFT) radical polymerization. The subscripts in the abbreviations indicate the degree of polymerization (DP). Furthermore, AMPS and APTAC were polymerized using a P(SA)91 macro-chain transfer agent to prepare an anionic diblock copolymer (P(SA)91S67) and a cationic diblock copolymer (P(SA)91A88), respectively. The DP was estimated from quantitative 13C NMR measurements. A stoichiometrically charge neutralized mixture of the aqueous P(SA)91S67 and P(SA)91A88 formed water-soluble polyion complex (PIC) micelles comprising PIC cores and amphoteric random copolymer shells. The PIC micelles were in a dynamic equilibrium state between PIC micelles and charge neutralized small aggregates composed of a P(SA)91S67/P(SA)91A88 pair. Interactions between PIC micelles and fetal bovine serum (FBS) in phosphate buffered saline (PBS) were evaluated by changing the hydrodynamic radius (Rh) and light scattering intensity (LSI). Increases in Rh and LSI were not observed for the mixture of PIC micelles and FBS in PBS for one day. This observation suggests that there is no interaction between PIC micelles and proteins, because the PIC micelle surfaces were covered with amphoteric random copolymer shells. However, with increasing time, the diblock copolymer chains that were dissociated from PIC micelles interacted with proteins

Thermo-Responsive Polyion Complex of Polysulfobetaine and a Cationic Surfactant in Water

Poly(4-((3-methacrylamidopropyl)dimethylammonium)butane-1-sulfonate) (PSBP) was prepared via controlled radical polymerization. PSBP showed upper critical solution temperature (UCST) behavior in aqueous solutions, which could be controlled by adjusting the polymer and NaCl concentrations. Owing to its pendant sulfonate anions, PSBP exhibited a negative zeta potential of −7.99 mV and formed a water-soluble ion complex with the cationic surfactant cetyltrimethylammonium bromide (CTAB) via attractive electrostatic interaction. A neutral PSBP/CTAB complex was formed under equimolar concentrations of the pendant sulfonate group in PSBP and the quaternary ammonium group in CTAB. Transmittance electron microscopic images revealed the spherical shape of the complex. The stoichiometrically neutral-charge PSBP/CTAB complex exhibited UCST behavior in aqueous solutions. Similar to PSBP, the phase transition temperature of the PSBP/CTAB complex could be tuned by modifying the polymer and NaCl concentrations. In 0.1 M aqueous solution, the PSBP/CTAB complex showed UCST behavior at a low complex concentration of 0.084 g/L, whereas PSBP did not exhibit UCST behavior at concentrations below 1.0 g/L. This observation suggests that the interaction between PSBP and CTAB in the complex was stronger than the interpolymer interaction of PSBP